Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:174159265-174159588 | Common:4; Rare:114 | ||||
chr1:174274935-174275115 | Rare:34 | ||||
chr1:174799589-174799791 | Rare:44 | ||||
chr1:174875420-174875532 | Rare:23 | ||||
chr1:174964547-174964814 | Rare:49 | ||||
chr1:174999292-174999492 | Common:2; Rare:57 | ||||
chr1:174999599-175000145 | Common:3; Rare:177 | ||||
chr1:175023404-175023626 | Common:1; Rare:60 | ||||
chr1:176207262-176207352 | Common:1; Rare:47 | ||||
chr1:178725029-178725347 | Common:10; Rare:109 | ||||
chr1:179293664-179293898 | Common:3; Rare:74 | ||||
chr1:179877756-179877905 | Rare:32 | ||||
chr1:179882474-179882908 | Rare:213; Clinvar:9; Clinvar (benign):2 | ||||
chr1:180502357-180502700 | Common:1; Rare:119 | ||||
chr1:180502824-180502957 | Rare:52 |